Skip to content

Effect of permissibility hypercapnia on postoperative delirium in elderly patients undergoing thoracoscopic radical resection of esophageal cancer

Effect of permissibility hypercapnia on postoperative delirium in elderly patients undergoing thoracoscopic radical resection of esophageal cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059008
Enrollment
Unknown
Registered
2022-04-22
Start date
2022-04-12
Completion date
Unknown
Last updated
2024-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative delirium

Interventions

Control group:PaCO2 was 35-45mmHg
Experimental group:PaCO2 was 46-55mmHg

Sponsors

Department of Anesthesiology, Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 65 years, no gender limit; 2. The pathological or cytological diagnosis was esophageal cancer, and thoracoscopic radical operation was planned; 3. ASA disease classification grade II-III; 4. Subjects understood and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. The score of MMSE scale is less than 24 points; 2. Have a second primary tumor; 3. Complicated with serious diseases, including severe liver and kidney function injury, autoimmune diseases, immune deficiency, cardiovascular and cerebrovascular diseases, neuropsychiatric diseases, blood diseases, etc.; 4. Patients with previous difficulties in endoscopic surgery (such as severe chronic obstructive pulmonary disease, acute inflammatory bowel disease, obesity, etc.); 5. Poor control of diabetes and hypertension; 6. Poor compliance, difficult to cooperate with treatment and follow-up; 7. Participated in other clinical studies in the last 3 months; 8. Situations in which other researchers found it inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Postoperative delirium;Cerebral oxygen;

Secondary

MeasureTime frame
Hemodynamics;Postoperative pain score;

Countries

China

Contacts

Public ContactHu Xianwen
xjw161915@163.com+86 15155159719

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026